Pasting paper made of glass fiber nonwoven comprising carbon graphite

ABSTRACT

Embodiments of the invention provide an absorptive glass mat (AGM) battery having a positive electrode, a negative electrode, and a nonwoven fiber separator positioned between the electrodes. The separator includes a mixture of glass fibers having diameters between about 8 μm to 13 μm and glass fibers having diameters of at least 6 μm and a silane sizing. An acid resistant binder bonds the glass fibers to form the separator. A wetting component is applied to the separator to increase the wettability such that the separator has or exhibits an average water wick height of at least 1.0 cm after exposure to water for 10 minutes. A conductive material is disposed on at least one surface of the separator such that when the separator is positioned adjacent an electrode, the conductive material contacts the electrode. An electrical resistance of less than 100,000 ohms per square enables electron flow about mat.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation in part application and claims thebenefit of copending U.S. patent application Ser. No. 14/045,579, filed,Oct. 3, 2013, and U.S. patent application Ser. No. 14/048,771, filedOct. 8, 2013, the complete disclosures of which are herein incorporatedby reference.

BACKGROUND OF THE INVENTION

Lead-acid batteries are characterized as being inexpensive and highlyreliable. As such, they are widely used as an electrical power sourcefor starting motor vehicles, golf carts, and other electric vehicles. Inrecent years, a variety of measures to improve fuel efficiency have beenconsidered in order to prevent atmospheric pollution and global warming.Examples of motor vehicles subjected to fuel-efficiency improvementmeasures that are being considered include idling stop vehicles (ISSvehicles) where the engine is stopped when the vehicle is not in motionto prevent unnecessary idling of the engine and to reduce engineoperation time.

In an ISS vehicle, the number of engine startup cycles is higher, andthe lead-acid battery discharges a large electrical current during eachstartup. In addition, the amount of electricity generated by thealternator in an ISS vehicle is smaller, and the lead-acid battery ischarged in an intermittent manner. As such, charging of the battery isoften insufficient. Stated differently, the battery is in a partiallycharged state known as a PSOC (i.e., partial state of charge).Accordingly, a lead-acid battery used in an ISS vehicle is required tohave a capability in which the battery is charged as much as possible ina relatively short time. In other words, the lead-acid battery shouldhave a higher charge acceptance. Therefore, improvements in the chargeacceptance of a lead-acid battery are desired.

Lead-acid batteries typically have a shorter lifespan when used underPSOC than in an instance in which the battery is used in a fully chargedstate. One reason for the shorter lifespan under PSOC is believed to bedue to repeatedly charging and recharging the battery in aninsufficiently charged state. Charging and recharging the battery inthis manner negatively affects the battery's electrodes or plates. Forexample, lead sulfate forms on the negative plate during discharge andundergoes progressive coarsening during charging and tends not to returnto metallic lead. Improving the charge acceptance may prevent thebattery from being charged and recharged in an insufficiently chargedstate, which may inhibit coarsening of lead sulfate due to repeatedcharging/discharging. This may increase the life span of the lead-acidbattery.

In addition, there are inherent disadvantages to lead-acid batteries.For example, during discharge of the lead-acid battery, the lead dioxide(a fairly good conductor) in the positive plate is converted to leadsulfate (an insulator). The lead sulfate can form an impervious layerencapsulating the lead dioxide particles which limits the utilization oflead dioxide often to less than 50 percent of capacity, and morecommonly around 30 percent. The low percentage of usage is a key reasonwhy the power and energy performance of a lead-acid battery isinherently less than optimum. It is believed that this insulator layerleads to higher internal resistance for the battery. Improving thecharge acceptance may also help reduce issues associated with formationof lead sulfate. In addition, lead-acid batteries having a separatortypically exhibit a voltage drop when operated in cranking cycles at lowoperating temperatures (multiple starting procedures). This disadvantagehinders the acceptance of such battery systems for a broader use.

BRIEF SUMMARY OF THE INVENTION

Embodiments of the invention provide an absorptive glass mat (AGM)battery. The battery may include a positive electrode, a negativeelectrode, and a nonwoven fiber mat separator positioned between thepositive electrode and the negative electrode. The nonwoven fiberseparator may include a mixture of glass fibers that may include aplurality of first glass fibers having diameters between about 8 μm to13 μm and a plurality of second glass fibers having diameters of atleast 6 μm. The plurality of second glass fibers may further include asilane material sizing. The nonwoven fiber separator may also include anacid resistant binder that bonds the plurality of first and second glassfibers to form the nonwoven fiber separator. The nonwoven fiberseparator may further include a wetting component applied to thenonwoven fiber separator to increase the wettability of the nonwovenfiber separator such that the nonwoven fiber separator has or exhibitsan average water wick height of at least 1.0 cm after exposure to waterfor 10 minutes conducted according to method ISO8787. The nonwoven fiberseparator may also include a conductive material disposed on at leastone surface of the nonwoven fiber separator such that when the nonwovenfiber separator is positioned adjacent the positive or negativeelectrode, the conductive material contacts the positive or the negativeelectrode. The nonwoven fiber separator may have an electricalresistance of less than about 100,000 ohms per square to enable electronflow about the nonwoven fiber separator.

In another embodiment, a nonwoven fiber separator for an AGM battery,the nonwoven fiber separator is provided. The nonwoven fiber separatormay include a mixture of glass fibers including a plurality of firstglass fibers having diameters between about 8 μm to 13 μm and aplurality of second glass fibers having diameters of at least 6 μm. Theplurality of second glass fibers may further include a silane materialsizing. The nonwoven fiber separator may also include an acid resistantbinder that bonds the plurality of first and second glass fibers to formthe nonwoven fiber separator. A wetting component may be applied to thenonwoven fiber separator to increase the wettability of the nonwovenfiber separator such that the nonwoven fiber separator has or exhibitsan average water wick height of at least 1.0 cm after exposure to waterfor 10 minutes conducted according to method ISO8787. The nonwoven fiberseparator may further include a conductive material disposed on at leastone surface of the nonwoven fiber separator such that when the nonwovenfiber separator is positioned adjacent a positive or a negativeelectrode of a lead-acid battery, the conductive material contacts thepositive or negative electrode. The nonwoven fiber separator may have anelectrical resistance of less than about 100,000 ohms per square toenable electron flow about the nonwoven fiber separator.

In another embodiment, a method of manufacturing a nonwoven fiberseparator for use in a lead-acid battery is provided. The method mayinclude providing a mixture of glass fibers including a plurality offirst glass fibers having diameters between about 8 μm to 13 μm and aplurality of second glass fibers having diameters of at least 6 μm. Theplurality of second glass fibers may also include a silane materialsizing. The method may also include applying an acid resistant binder tothe mixture of glass fibers to couple the mixture of glass fiberstogether to form the nonwoven fiber separator. The method may furtherinclude applying a conductive material to at least one surface of thenonwoven fiber separator such that when the nonwoven fiber separator ispositioned adjacent a positive or a negative electrode of a battery, theconductive material contacts the positive or the negative electrode. Thenonwoven fiber separator may have an electrical resistance of less thanabout 100,000 ohms per square so as to enable electron flow about thenonwoven fiber separator. The method may additionally include applying awetting component to the nonwoven fiber separator to increase thewettability of the nonwoven fiber separator such that the nonwoven fiberseparator has or exhibits an average water wick height of at least 1.0cm after exposure to water for 10 minutes conducted according to methodISO8787.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is described in conjunction with the appendedfigures:

FIG. 1 illustrates an exploded perspective view of a battery cellassembly.

FIG. 2 illustrates an assembled cross section view of the battery cellassembly of FIG. 1.

FIGS. 3A-3C illustrate cross section views of various configurations ofan electrode or plate and a nonwoven fiber mat.

FIG. 4 illustrates a process for preparing an electrode or plate havinga nonwoven fiber mat disposed on or near a surface of the electrode orplate.

FIG. 5 illustrates a method of manufacturing a plate of a lead-acidbattery.

FIG. 6 illustrates a method of manufacture of a nonwoven fiber materaccording to embodiments of the invention.

In the appended figures, similar components and/or features may have thesame numerical reference label. Further, various components of the sametype may be distinguished by following the reference label by a letterthat distinguishes among the similar components and/or features. If onlythe first numerical reference label is used in the specification, thedescription is applicable to any one of the similar components and/orfeatures having the same first numerical reference label irrespective ofthe letter suffix.

DETAILED DESCRIPTION OF THE INVENTION

The ensuing description provides exemplary embodiments only, and is notintended to limit the scope, applicability or configuration of thedisclosure. Rather, the ensuing description of the exemplary embodimentswill provide those skilled in the art with an enabling description forimplementing one or more exemplary embodiments. It being understood thatvarious changes may be made in the function and arrangement of elementswithout departing from the spirit and scope of the invention as setforth in the appended claims.

Specific details are given in the following description to provide athorough understanding of the embodiments. However, it will beunderstood by one of ordinary skill in the art that the embodiments maybe practiced without these specific details. For example, processes, andother elements in the invention may be shown as components in blockdiagram form in order not to obscure the embodiments in unnecessarydetail. In other instances, well-known processes, structures, andtechniques may be shown without unnecessary detail in order to avoidobscuring the embodiments.

Also, it is noted that individual embodiments may be described as aprocess which is depicted as a flowchart, a flow diagram, a data flowdiagram, a structure diagram, or a block diagram. Although a flowchartmay describe the operations as a sequential process, many of theoperations can be performed in parallel or concurrently. In addition,the order of the operations may be re-arranged. A process may beterminated when its operations are completed, but could have additionalsteps not discussed or included in a figure. Furthermore, not alloperations in any particularly described process may occur in allembodiments. A process may correspond to a method, a function, aprocedure, a subroutine, a subprogram, etc. When a process correspondsto a function, its termination corresponds to a return of the functionto the calling function or the main function.

The ensuing description provides exemplary embodiments only, and is notintended to limit the scope, applicability or configuration of thedisclosure. Rather, the ensuing description of the exemplary embodimentswill provide those skilled in the art with an enabling description forimplementing one or more exemplary embodiments. It being understood thatvarious changes may be made in the function and arrangement of elementswithout departing from the spirit and scope of the invention as setforth in the appended claims.

Embodiments of the invention provide nonwoven fiber mats (hereinafterreinforcement mat) that have an electrically conductive surface thatenhances electron flow to and/or from the battery plates, as well asincluding a wetting component to improve the wettability of the mats.The reinforcement mats may be used to reinforce plates in lead-acidbatteries, or other batteries, or used on separators positioned betweenelectrodes, e.g. in Absorptive Glass Mat (AGM) battery applications. Thereinforcement mats can be any woven or, preferably, any nonwoven matwhich is acid resistant, such as glass mat, or mat made from mainlypolyolefin fibers, or mixture of polyolefin and glass fibers.

In some embodiments, the electron flow is enhanced by providing a mathaving a conductive surface or surfaces and/or other conductive pathway.The enhanced electron flow extends the battery's life, especially inlead acid batteries where continual discharge and recharge of thebattery results in degradation of the battery's electrodes. For example,during discharge of the lead acid battery, lead dioxide (a goodconductor) in the positive electrode plate is converted to lead sulfate,which is generally an insulator. The lead sulfate can form an imperviouslayer or layers encapsulating the lead dioxide particles, which maylimit the utilization of the lead dioxide, and thus the battery, to lessthan 50 percent of capacity, and in some cases about 30 percent. Theinsulative lead sulfate layer may also lead to higher resistance for thebattery. The effect may be a decrease in the electrical current providedby the battery and/or in the discharge life of the battery. In someembodiments, the mat may offer a significant improvement (decrease) ofthe voltage drop when operated in cranking cycles at low operatingtemperatures (multiple starting procedures) if compared to existingsystems. Conductive reinforcement mats may replace other platereinforcement means, such as paper, that are currently used in lead-acidor other batteries. The conductive reinforcement mat provides severaladvantages over the current plate reinforcement means, such as notdissolving in the electrolyte (e.g., sulfuric acid); providing vibrationresistance, reducing plate shedding, strengthening or reinforcing theplate; and/or providing good dimensional stability, which may alloweasier guiding or handling during battery plate manufacturing processes.

In regards to the conductive properties of the conductive reinforcementmat, the electrically conductive surface of the mat may provide anadditional route for electron flow. The route provided by the mat istypically separate from the route provided by the conductor plate orgrid of the battery. The multiple electron paths (e.g., the mat andconductor plate) allows the electrons to flow via either or both theconductive reinforcement mat or the conductor plate/grid depending onwhich route provides the least electrical resistance. In this manner, asthe electrode degrades due to formation of lead sulfate, numerous routesfor the electrons are maintained, thereby extending the overall life ofthe battery. In some embodiments, the battery may include a batteryseparator that also includes a conductive material. The batteryseparator may provide extra electron flow routes in addition to thefiber mat and conductor plate or grid. Such a separator may beparticularly useful in AGM batteries discussed herein. In someembodiments, the separator may include a non-conductive separatinglayer.

The conductive reinforcement mat also provides excellent plate orelectrode reinforcement due to their excellent strength properties. Theconductive reinforcement mat may also have a relatively small ordecreased mat size. The relatively thin fiber mats reduce the overallvolume that the mat occupies, which allows an increased amount ofelectrolyte and/or active material paste to be used within the lead-acidbattery. The thinner mats also improve processing efficiency byincreasing the mat footage on the processing rolls, which reduces thefrequency of roll changing. In some embodiments, the conductivereinforcement mat may be less than 10 mils thick (i.e., 0.010 inches or254 μm), and more commonly less than 9 mils thick (i.e., 0.009 inches).In one embodiment, the conductive reinforcement mat is about 6 mils and8 mils or between about 6 mils and 7 mils thick.

In some embodiments, the conductive reinforcement mats may include acombination of electrically insulative fibers and a conductive material.The mat made of these electrically insulative fibers may have anelectrical resistance greater than about 1 million ohms per square(sheet resistance). In one embodiment, the electrically insulativefibers may include glass fibers, polyolefin fibers, polyester fibers,and the like. For convenience in describing the embodiments, thedisclosure herein will describe mainly glass fibers, although it shouldbe realized that other electrically insulative fibers may be used.

The electrically conductive material may include a layer or mat ofconductive fibers or a layer of other conductive materials, such as ametallic sheet or film that is positioned atop the electricallyinsulative fiber layer. In many embodiments, the conductive material isa non-metal material. In some embodiments, the conductive material mayinclude a coating of conductive material applied to or atop the fibermat. In a specific embodiment, the conductive material may be added to abinder material that is applied to the plurality of insulative fibersduring manufacture of the fiber mat, or that is sprayed atop apreviously manufactured fiber mat. The conductive material may includeconductive polymers (e.g., polyanilines), carbon material (e.g., carbonblack, activated carbon, graphite, carbon nanofibers, carbon nanotubes,graphene, CNS (carbon nanostructure)), and the like. In a specificembodiment, the conductive material may include conductive fibers thatare disposed at least partially within and/or entangled with a fiber mathaving the insulative fibers. The conductive fibers may be mixed withthe insulative fibers (e.g., glass fibers, polymeric fibers, and thelike) to make a mat that is conductive. In an exemplary embodiment,graphene or CNS may be used due to their high electrical conductivityand inertness to sulfuric acid. CNS may be more commonly used since itcan be readily dispersed in water.

The conductive reinforcement mat is typically positioned within thebattery so that the electrically conductive material/layer contacts theactive paste of the battery's electrodes. The conductive layer mat maybe disposed across substantially the entire surface of the conductivereinforcement mat so that the electrically conductive layer issubstantially equal in size and shape to the conductive reinforcementmat. In this manner the electrically conductive layer provides a largeconductive surface that contacts the electrode.

The conductive reinforcement mats may have a total tensile strength ofat least 30 lbs/3 inch and more commonly at least 35 lbs/3 inch. Toachieve this tensile strength, the nonwoven fiber mat may have a tensilestrength in the machine direction of at least 22 lbs/3 inch and atensile strength in the cross-machine direction of at least 13 lbs/3inch. The description of “lbs/3 inch” generally refers to a method oftesting the mat strength where a 3 inch by 12 inch rectangular piece ofthe fiber mat is subjected to a tensile stress until the mat fails, suchas by ripping or tearing. Mats having tensile strengths less than 22lbs/3 inch in the machine direction and less than 13 lbs/3 inch in thecross-machine direction may not have sufficient strength to withstandwinding and rewinding during processing and/or to reinforce plates of alead-acid or other battery.

In some embodiments, the conductive reinforcement mats may include ablend of two or more different sized coarse diameter fibers. Thedescription of coarse diameter fibers generally includes fibers rangingin diameter between about 6 μm and about 30 μm in one embodiment, andbetween about 8 μm and about 20 μm in another embodiment. For example,in one embodiment, a conductive reinforcement mat may include a blend offirst glass fibers having fiber diameters in the range of between 8 μmand 13 μm and second glass fibers having fiber diameters at least about6 μm. The preferred diameter range is between 6 μm and 7 μm. In someembodiments, the second glass fibers may include a silane materialsizing to provide increased adhesive properties and/or acid resistance.In one embodiment, the nonwoven fiber mats include at least 25% of eachof the first and second glass fibers. The glass fibers typically havefiber lengths that range between about ⅓ of an inch to about 1½ inches,although fiber lengths are more commonly about ⅓ inch to ¾inch or 1inch.

The conductive reinforcement mats also include a binder that bonds theglass fibers together, and that bonds the conductive fibers to the glassfibers when conductive fibers are employed as the conductive material.The binder is typically applied to the glass fibers so that the bindercomprise between about 5% and 45% by weight of the conductivereinforcement mats, between about 15% and 35% by weight of theconductive reinforcement mats, and more commonly comprises between about5% and 30% by weight of the conductive reinforcement mats. The binder isgenerally an acid and/or chemically-resistant binder (e.g., an acrylicbinder) that delivers the durability to survive in the acid environmentthroughout the life of the battery and the strength to survive the platepasting operation. In a specific embodiment, the binder may also includethe conductive material. For example, the conductive material (e.g.,grapheme, graphite powder, and the like) may be dispersed within thebinder.

According to one embodiment, a fiber mat (e.g., glass fiber mat) may becoated with the conductive material to form the conductive reinforcementmat. This may be achieved via dip-coating, curtain coating, spraying,dip-and-squeeze techniques, and the like. In another embodiment, theconductive material may be mixed with the binder and applied on thefiber mat during the binder application. The latter process represents a“one-step” or single application process. The binder may help bond theconductive material to the mat. Having described several embodiments ofthe invention, additional aspects will be more apparent with referenceto the figures described below.

In some embodiments, the conductive material of the reinforcement matmay be non-metal. The non-metal conductive material coated mat may beused for reinforcing electrode plates and can provide benefits describedherein, such as improving electron transfer and current output, reducinginternal resistance of the battery, improving charging acceptance, andthe like. It is believed that by using a non-metal conductive materialcoated mat either as a separator support mat or plate reinforcement mat,the electrons do not have to go through the electrode spot where ahigher resistance exists (e.g., due to micro-cracks and the like). Theelectrons can flow freely on the conductive surface of the mat andchoose the contacting spot having minimum resistance. This benefitbecomes more pronounced after the battery is used for an extend periodof time.

In addition to having conductive properties, reinforcement mats can alsoprovide a wicking capability to allow a complete wetting of theelectrodes. Such mats may also aid in the drying of the plate/electrodeafter the plate/electrode is pasted with a lead paste slurry. The term“wettability” as used herein refers to the mats ability to wick orotherwise transport water and/or other solutions, such as a water andacid solution, from a location. For example, in testing the wettabilityor wickability of glass fiber mats, a strip of the mat, which is oftenabout 1 inch in width, 6 inches long, and typically 0.1-3 mm thick, maybe dipped vertically in water or another solution for a given amount oftime, such as 10 minutes. The distance or height the water absorbswithin the glass fiber mat from a surface of the water or other solutionindicates the mat's ability to wick or otherwise transport the water orsolution. The test to determine the average water wick height of thereinforcement mat may be conducted according to method ISO8787. In someembodiments, the wicking capability may also improve the wetting of theelectrode with electrolyte.

The mats described herein increase the wettability of glass fiber matsby adding a wetting component to the glass fiber mats. The added wettingcomponent provides an avenue for the water and/or water/acid solution toevaporate. In one embodiment, the added wetting component aids in thetransport of water and/or water/acid solution to a surface of the matwhere the water and/or water/acid solution may evaporate. In someembodiments, the combination of the first glass fibers, second glassfibers, and wetting component may provide 4-5 times the wettability of astandard mat.

In one embodiment, the added wetting component may be a wettablecomponent of an acid resistant binder that is used to bond the glassfibers of the mat together. The wettable component may be a hydrophilicfunctional group that increases the ability of the water and/orwater/acid solution to absorb within the glass mat or flow along asurface of the glass mat. In other embodiments, wettable component maybe a hydrophilic binder that is blended or combined with the acidresistant binder to form a binder mixture. In some embodiments, thewettable component may include starch, cellulose, stabilized cotton, ahydrophilic binder (e.g., a poly acrylic acid based binder) and thelike. In some embodiments, the binder may protect the wettablecomponent, such as cotton, from deterioration. In some embodiments, theglass mat may include only coarse glass fibers, or fibers having a fiberdiameter of between about 6 and 30 μm. The wettable component mayincrease such mat's ability to absorb the water and/or water/acidsolution and/or allow the water and/or water/acid solution to flowessentially along a surface of the reinforcement mat.

As used herein, the term hydrophilic (or acidophilic) binder refers to abinder having a contact angle with water (or a 33 wt. % sulfuric acidmedium for acidophilic) of less than about 90°, preferably less than70°, and most preferably less than 50°. In testing the contact angle ofthe binder, the binder may be spin-coated on a glass slide and thencured before being exposed to the above solution to measure the contactangle.

In some embodiments, the binder and wettable component may be added tothe mat up to about 20% LOI (Loss on Ignition). In other embodiments, afirst binder that does not include a wettable component may be used tobond the coarse glass fibers, and a second binder having the wettablecomponent (e.g., a hydrophilic functional group) may be applied to themat to increase the wettability of the mat. The first and second bindersmay be mixed or combined together to form a single binder mixture thatis applied to the coarse glass fibers.

In another embodiment, the added wetting component may be a fiber. Thefiber may be a natural fiber, such as cellulose or stabilized cotton, orcan be a synthetic fiber such as polyester, or can include a mixture ofnatural and/or synthetic fibers (hereinafter component fibers).Stabilized cotton include cotton filaments that are coated with an acidresistant binder and/or embedded in such a binder. The component fibersmay have a microfiber structure, or in other words may have fiberdiameters between about 0.01 and 10 μm, more often between about 0.5 and3 μm. The wickability/wettability of the component fibers may be betterthan the glass fibers (e.g., coarse fibers in the range of 6-30 μm) dueto the dimensions of the fibers (e.g., microfibers) and/or because thecomponent fibers typically include hydrophilic functional groups, suchas OH groups, COOH groups, and the like.

In some embodiments, the component fibers may be formed into a mat thatis separate from the mat of glass fibers, such as by applying thecomponent fibers atop a glass fiber mat. The component fiber mat may bebonded with the glass fiber mat so that the resulting combined mat hasessentially two layers—a layer of glass fibers and a layer of componentfibers. In some embodiments, a second component fiber mat may be bondedto an opposite side of the glass fiber mat so that the resultingcombined mat has essentially three layers—a glass mat sandwiched betweentwo component fiber mats. In another embodiment, the component fibersmay be mixed with the glass fibers so that the resulting mat includes acombination of entangled glass fibers and component fibers. An acidresistant binder may be used to bond the component fiber mat with theglass fiber mat, or may be used to bond the entangled glass fibers andcomponent fibers to form the reinforcement mat.

In one embodiment, the glass fiber mat may include mainly coarse fibers,or fibers having a fiber diameter of between about 6 and 30 μm. In someembodiments, other acid resistant fibers may be used instead of glassincluding polyethylene fibers, polypropylene fibers, polyester fibers,and the like. The component fibers (e.g. cellulose fibers) provide thereinforcement mat with good wetting properties by aiding in thetransport of water and or a water/acid solution to the surface of thereinforcement mat where the water and/or water/acid solution mayevaporate.

In another embodiment, the glass fiber mat may include mainly glassmicrofibers, or fibers having a fiber diameter of between about 0.01 and5 μm. The resulting reinforcement mat may include mainly or only glassmicrofibers that are entangled with the components fibers, or that arebonded with a component fiber mat(s). Such a reinforcement mat may haveexceptional wetting and wicking capabilities.

In some embodiments, the reinforcement mat may include a combination ofcoarse acid resistant fibers (e.g., fibers having a fiber diameter ofbetween 6 and 30 μm), acid resistant microfibers (e.g., fibers having afiber diameter of between 0.01 and 5 μm), and the component fibers. Theacid resistant coarse fibers and microfibers are commonly glass fibers,although other acid resistant fibers may be used. In some embodiments,the reinforcement mat may include between about 15-85% of thecombination of glass coarse and microfibers, and between about 15-85% ofthe component fibers. In another embodiment, the reinforcement mat mayinclude between about 40-60% of the coarse glass fibers, 20-30% of theglass microfibers, and 20-30% of the component fibers. The componentfibers and microfibers may function synergistically to wick water and/orthe water/acid solution, and thus, may greatly improve thewettability/wickability of the reinforcement mat. For example, glassmicrofibers are typically more wettable than coarse glass fibers. Themicrofibers, however, may be covered or concealed by the coarse glassfibers and/or binder and, thus, not exposed to the water and/orwater/acid solution.

In some embodiments, the binder having the wettable component (e.g., ahydrophilic functional group) may be used to bond a reinforcement matthat includes the coarse glass and component fibers, or that includesthe coarse glass fibers, glass microfibers, and component fibers. Thewettable component may further increase the wettability of thereinforcement mats, such as by providing another avenue for transport ofthe water and/or water/acid solution and/or by increasing the exposureof the water and/or water/acid solution to the glass microfibers.

In another embodiment, the added wetting component may be a wettablesolution that is added to the reinforcement mat. The wettable solutionmay be added to the reinforcement mat so as to saturate thereinforcement mat, or so as to be disposed on at least one surface ofthe reinforcement mat after drying of the wettable solution. Thewettable solution may include a starch solution, cellulose solution,polyvinyl alcohol solution, polyacrylic acid solution, and the like. Thewettable solution may be added to the mat after the mat is formed, suchas by dip-coating the reinforcement mat in the wettable solution, or byapplying the wettable solution via spray coating, curtain coating, andthe like. After application of the wettable solution, the wettablesolution may be dried to provide an avenue for the water and/orwater/acid solution to evaporate. The wettable solution may subsequentlydissolve when exposed to an acid environment, such as the environment ofthe battery's electrolyte, so that the reinforcement mat remainsadjacent the electrode after dissolving of the wettable solution.

According to any of the embodiments described herein, the addition ofthe wetting component to the reinforcement mat may increase thewettability of the reinforcement mat such that the reinforcement matexhibits an average water wick height of at least 1.0 cm after exposureto water for 10 minutes. The test to determine the average water wickheight of the reinforcement mat may be conducted according to methodISO8787. Similarly, the addition of the wetting component to thereinforcement mat may enable the reinforcement mat to exhibit an averagewater/acid solution wick height of at least 1.0 cm after exposure to thewater/acid solution for 10 minutes. This test is similarly conductedaccording to method ISO8787. In other embodiments, the average waterwick height and/or water/acid solution wick height may be at least 0.8cm after exposure to the respective solution for 10 minutes. In yetother embodiments, the average water wick height and or water/acidsolution wick height may be greater than 1 cm after exposure to therespective solution for 10 min. As briefly described above, the additionof silane sized glass microfibers to the reinforcement mat maysignificantly increase the wettability/wickability of the reinforcementmat such that the average water wick height and/or water/acid solutionwick height increases.

Embodiments

FIGS. 1 and 2, respectively, show a perspective exploded view of alead-acid battery cell 200 and a cross-section assembled view of thelead-acid battery cell 200. The lead-acid batter cell 200 may representa cell used in either flooded lead-acid batteries or Absorptive GlassMat (AGM) batteries. Each cell 200 may provide an electromotive force(emf) of about 2.1 volts and a lead-acid battery may include 3 suchcells 200 connected in series to provide an emf of about 6.3 volts ormay include 6 such cells 200 connected in series to provide an emf ofabout 12.6 volts, and the like. Cell 200 includes a positive plate orelectrode 202 and a negative plate or electrode 212 separated by batteryseparator 220 so as to electrically insulate the electrodes 202 and 212.Positive electrode 202 includes a grid or conductor 206 of lead alloymaterial. A positive active material 204, such as lead dioxide, istypically coated or pasted on grid 206. Grid 206 is also electricallycoupled with a positive terminal 208. Grid 206 provides structuralsupport for the positive active material 204 along with electricalconductivity to terminal 208.

Likewise, negative electrode 212 includes a grid or conductor 216 oflead alloy material that is coated or pasted with a negative activematerial 214, such as lead. Grid 216 is electrically coupled with anegative terminal 218. Like grid 206, grid 216 structurally supports thenegative active material 214 along with providing electrical conductanceto terminal 218. In flooded type lead-acid batteries, positive electrode202 and negative electrode 212 are immersed in an electrolyte (notshown) that may include a sulfuric acid and water solution. In AGM typelead-acid batteries, the electrolyte is absorbed and maintained withinbattery separator 220. Battery separator 220 is positioned betweenpositive electrode 202 and negative electrode 212 to physically separatethe two electrodes while enabling ionic transport, thus completing acircuit and allowing an electronic current to flow between positiveterminal 208 and negative terminal 218. Separator 220 typically includesa microporous membrane (i.e., the solid black component), which is oftena polymeric film having negligible conductance. The polymeric film mayinclude micro-sized voids that allow ionic transport (i.e., transport ofionic charge carriers) across separator 220. In one embodiment, themicroporous membrane or polymeric film may have a thickness of 50micrometers or less, and preferably 25 micrometers or less, may have aporosity of about 50% or 40% or less, and may have an average pore sizeof 5 micrometers or less and preferably 1 micrometer or less. Thepolymeric film may include various types of polymers includingpolyolefins, polyvinylidene fluoride, polytetrafluoroethylene,polyamide, polyvinyl alcohol, polyester, polyvinyl chloride, nylon,polyethylene terephthalate, and the like. Separator 220 may also includeone or more fiber mats that are positioned adjacent one or both sides ofthe microporous membrane/polymeric film to reinforce the microporousmembrane and/or provide puncture resistance.

Positioned near a surface of negative electrode 212 is a nonwoven fibermat 230 (referred to herein as a reinforcement mat). Reinforcement mat230 is disposed partially or fully over the surface of negativeelectrode 212 so as to partially or fully cover the surface. As shown inFIGS. 3A-3C, a reinforcement mat 230 may be disposed on both surfaces ofthe negative electrode 212, or may fully envelope or surround theelectrode. Likewise, although reinforcement mat 230 is shown on theouter surface of the electrode 212, in some embodiments reinforcementmat 230 may be positioned on the inner surface of the electrode 212(i.e., adjacent separator 220). Reinforcement mat 230 reinforces thenegative electrode 212 and provides an additional supporting componentfor the negative active material 214. The additional support provided byreinforcement mat 230 may help reduce the negative effects of sheddingof the negative active material particles as the active material layersoftens from repeated charge and discharge cycles. This may reduce thedegradation commonly experienced by repeated usage of lead-acidbatteries.

Reinforcement mat 230 is often impregnated or saturated with thenegative active material 214 so that the reinforcement mat 230 ispartially or fully disposed within the active material 214 layer.Impregnation or saturation of the active material within thereinforcement mat means that the active material penetrates at leastpartially into the mat. For example, reinforcement mat 230 may be fullyimpregnated with the negative active material 214 so that reinforcementmat 230 is fully buried within the negative active material 214 (i.e.,fully buried within the lead paste). Fully burying the reinforcement mat230 within the negative active material 214 means that the mat isentirely disposed within the negative active material 214. In oneembodiment, reinforcement mat 230 may be disposed within the negativeactive material 214 up to about a depth X of about 20 mils (i.e., 0.020inches) from an outer surface of the electrode 212. In otherembodiments, the glass mat 230 may rest atop the negative activematerial 214 so that the mat is impregnated with very little activematerial. Often the reinforcement mat 230 will be impregnated with thenegative active material 214 so that the outer surface of the mat formsor is substantially adjacent the outer surface of the electrode 212 (seereinforcement mat 240). In other words, the active material may fullypenetrate through the reinforcement mat 230 so that the outer surface ofthe electrode 212 is a blend or mesh of active material andreinforcement mat fibers.

As described herein, reinforcement mat 230 includes a plurality of glassfibers, an acid resistant binder that couples the plurality of glassfibers together to form the reinforcement mat. Reinforcement mat 230 mayhave an area weight of between about 10 and 100 g/m², more often betweenabout 20 and 60 g/m². Reinforcement mat 230 may be used for reinforcinga plate or electrode of a lead-acid battery and may include a relativelyhomogenous mixture of coarse glass fibers that may include a pluralityof first glass fibers having a diameter between about 8-13 μm and aplurality of second fibers having a diameter of at least 6 μm. As usedherein, relatively homogenous means that the mixture is at least 85%homogenous. In some embodiments the relatively homogenous mixture maymake up between about 70-95% of the mass of the mat 230. In someembodiments, the homogenous mixture may also include 5-30% conductivefibers. For example, conductive fibers having diameters between about 6and 8 μm and having lengths between about 8 and 10 mm can be included inthe relatively homogenous mixture. The reinforcement mat 230 alsoincludes an acid resistant binder that bonds the plurality of first andsecond glass fibers together to form the reinforcement mat 230. Thereinforcement mat 230 further includes a wetting component that isapplied to reinforcement mat 230 to increase the wettability/wickabilityof the reinforcement mat 230. The wettability/wickability of thereinforcement mat 230 may be increased such that the reinforcement mat230 has or exhibits an average water wick height and/or water/acidsolution wick height of at least 1.0 cm after exposure to the respectivesolution for 10 minutes in accordance with a test conducted according tomethod ISO8787.

Reinforcement mat 230 may include a conductive material so as to makereinforcement mat 230 electrically conductive. For example, a conductivelayer may be formed on one or more sides of reinforcement mat 230 byapplying a conductive material to at least one surface of reinforcementmat 230 or throughout reinforcement mat 230. The conductive layer may bepositioned to face and contact electrode 212 to provide electricalpathways along which the electrons may flow. The conductive materialcontacts the electrode 212, and more specifically the active material ofelectrode 212 to enable electron flow on a surface or throughreinforcement mat 230. The conductive material and/or layer ofreinforcement mat 230 may have an electrical resistance of less thanabout 100,000 ohms per square and more commonly less than about 50,000ohms per square so as to enable or enhance electron flow on the surfaceof the mat 230. In some embodiments, the conductive layer ofreinforcement mat 230 may be electrically coupled with a negativeterminal 218 to provide a route or path for current flow to terminal218.

As described herein, electrons may flow along either reinforcement mat230 or grid/conductor 216 depending on which conductive surface providesan electrical path of least electrical resistance. For example,electrons proximate to terminal 218 may flow along an electrical path ofgrid/conductor 216 while electrons distal to terminal 218 may flow alongan electrical path of reinforcement mat 230 due to a buildup of leadsulfate on grid/conductor 216 at the distal location.

In one embodiment, the conductive layer of reinforcement mat 230 may beformed on a surface of electrically insulative fibers (e.g., glassfibers) by coating the conductive material onto the insulative fibers orby spraying the conductive material on the surface of reinforcement mat230. In a specific example, the conductive material may be added to aprimary binder material that is applied to the wet-laid insulativefibers to couple the fibers together. The primary binder/conductivematerial mixture and wet-laid insulative fibers may then be cured sothat the conductive material completely coats or is saturated throughoutreinforcement mat 230 to form the conductive layer. In anotherembodiment, reinforcement mat 230 may be manufactured in a standardprocess where a primary binder without the conductive material isapplied to the wet-laid insulative fibers to couple the fibers together.The conductive material may then be dispersed in a secondary or dilutebinder that is then coated or sprayed onto the surface of reinforcementmat 230. Reinforcement mat 230 may then be cured so that the conductivematerial forms a conductive layer across the entire surface, or adefined portion, of reinforcement mat 230. In this embodiment, amajority of the conductive material may be positioned atop the surfaceof reinforcement mat 230.

In another embodiment, a reinforcement mat 230 may be manufacturedaccording to known processes. A catalyst may be subsequently added to asurface of reinforcement mat 230 and metal ions, such as copper, may begrown on the surface of the reinforcement mat via the applied catalyst.In still another embodiment, the conductive material may be added toreinforcement mat 230 via chemical vapor deposition processes.

In lead-acid battery environments, the conductive material used forreinforcement mat 230 should be relatively corrosion resistant due tothe aggressive electrochemical environment of the battery. In someembodiments, the conductive material may include a metal, a nanocarbon,graphene, graphite, a conductive polymer (e.g., polyanilines),nanocarbons or carbon nanotubes, carbon fibers, copper, titanium oxides,vanadium oxides, tin oxides, and the like. In a specific embodiment, theconductive material may include carbon nano-platelets, such as graphene.The graphene may be added to the primary binder or secondary/dilutebinder as described above and applied to reinforcement mat 230 (e.g., aglass or polyolefin fiber mat) between about 0.01% and 50% by weight, orin some embodiments between about 1% and 25% by weight. When cured, thecoating of graphene forms a conductive layer across the entire surface,or a defined portion, of reinforcement mat 230.

In another embodiment, the conductive layer may comprise a conductivefiber mat, foil, or screen that is positioned adjacent the surface ofreinforcement mat 230 or entangled with the electrically insulativefibers (e.g., glass fibers) of reinforcement mat 230. In one embodiment,the conductive layer may be made by coating or spraying the conductivefibers on the surface of reinforcement mat 230. In another embodiment, aconductive fiber mat may include a plurality of conductive fibersarranged in a non-woven or woven pattern and coupled together via abinder. The conductive fiber mat may be coupled with reinforcement mat230 via a binder and the like. Electrons may flow along the conductivefiber mat, foil, or screen as described herein, such as up to negativeterminal 218.

As briefly described above, reinforcement mat 230 may include aplurality of electrically insulative fibers, such as glass, polyolefin,polyester, and the like, which are primarily used to reinforce theelectrode. Because the reinforcement mat 230 is made of such insulativefibers, the reinforcement mat 230 may be essentially non-conductiveprior to or without the addition of the conductive material. Forexample, without combining or adding the conductive material/layer, thereinforcement mat 230 may have an electrical resistance greater thanabout 1 Megohm per square. In manufacturing the reinforcement mat 230,water or another liquid may be removed (e.g., via a vacuum) from asuspension of the fibers in the liquid medium. A binder may then beapplied to the wet-laid non-woven glass or polyolefin fibers to formreinforcement mat 230. As described previously, in some embodiments, theconductive material or fibers may be added to the binder and/or to theliquid medium. In one embodiment, reinforcement mat 230 may have athickness of between about 50 micrometers and about 500 micrometers andhave an average pore size of between about 5 micrometers and about 5millimeters.

The reinforcement mat 230 also includes a wetting component that isapplied to the reinforcement mat to increase the wettability/wickabilityof the reinforcement mat. The wettability/wickability of thereinforcement mat 230 is increased so that the reinforcement mat has orexhibits an average water wick height and/or average water/solution wickheight of at least 0.5 cm after exposure to the respective solution for10 minutes in accordance with a test conducted according to methodISO8787.

As described herein, the wetting component may be a wettable componentof the acid resistant binder (e.g., a hydrophilic functional group), ahydrophilic binder that is mixed with the acid resistant binder, thewetting component may be component fibers (e.g., cellulose or naturalfibers) that are bonded with the glass fibers of the reinforcement mat230, or the wetting component may be a wettable solution (e.g., starchor cellulose solution) that is applied to the reinforcement mat 230 suchthat the wettable solution saturates the reinforcement mat 230 or isdisposed on at least one surface of the reinforcement mat 230 upondrying of the wettable solution. In some embodiments, the wettingcomponent may include a combination of any of the aforementionedcomponents, such as a combination of cellulose fibers and an acidresistant binder having a wettable component. In a specific embodiment,the glass fibers of reinforcement mat 230 include first fibers havingfiber diameters between about 6 μm and about 30 μm, or 8 μm and about12, μm and second fibers having fiber diameters of at least about 6 μm.

As described herein, in some embodiments the wetting component may bewettable component of the acid resistant binder (e.g., a hydrophilicfunctional group) or a hydrophilic binder that is mixed/combined withthe acid resistant binder. In other embodiments, the wetting componentmay be a wettable solution (e.g. starch or cellulose solution) that isapplied to the reinforcement mat 230 so that the wettable solutionsaturates the reinforcement mat 230 or is disposed on at least onesurface of the reinforcement mat 230 after the wettable solution isdried. In still another embodiment, the wetting component may be aplurality of component fibers (e.g., cellulose, cotton, other naturalfibers, polyester, other synthetic fibers, or a combination of naturaland/or synthetic fibers) that are bonded with the reinforcement mat 230.According to one embodiment, the component fibers may form a componentfiber mat that is bonded to at least one side of the glass reinforcementmat 230 such that the reinforcement mat 230 comprises a two layer matconfiguration. In another embodiment, the component fibers may be mixedwith the glass fibers such that upon forming the glass mat the componentfibers are entangled with and bonded to the glass fibers. In yet otherembodiments, the wetting component may be a combination of the abovedescribed wetting components (i.e., a binder having a wettablecomponent, a wettable solution, and/or a component fiber).

Referring now to FIGS. 3A-C, illustrated are variouselectrode-reinforcement mat configurations. FIG. 3A illustrates aconfiguration where an electrode 300 has a single reinforcement mat 302disposed on or near an outer surface. As described above, reinforcementmat 302 may include a conductive material and/or layer so as to enableelectron flow on a surface and/or through reinforcement mat 302 to abattery terminal. Reinforcement mat 302 may also include a wettingcomponent as described above to provide the mat 302 with enhancedwettability characteristics. Reinforcement mat 302 may partially orfully cover the outer surface of electrode 300. The configuration ofFIG. 3B is similar to that of FIG. 3A except that an additionalreinforcement mat 304 is disposed on or near an opposite surface ofelectrode 300 so that electrode 300 is sandwiched between the two glassmats, 302 and 304. Either or both reinforcement mats, 302 and 304, mayinclude a conductive material and/or layer to enable electron flow to abattery terminal as well as a wetting component. As such, electrode 300may be sandwiched between two conductive reinforcement mats 302 and 304.FIG. 3C illustrates a configuration where a reinforcement mat 306envelopes or surrounds electrode 300. Although FIG. 3C illustrates thereinforcement mat 306 fully enveloping the electrode 300, in manyembodiments a top side or portion of the mat 306, or a portion thereof,is open. Glass mat 306 may include the conductive material and/or layeras described above to enable electron flow as well as a wettingcomponent.

Referring back to FIGS. 1 and 2, positioned near a surface of positiveelectrode 202 is a reinforcement mat 240. Reinforcement mat 240 may bearranged and/or coupled with positive electrode 202 similar to thearrangement and coupling of reinforcement mat 230 with respect tonegative electrode 212. For example, reinforcement mat 240 may bedisposed partially or fully over the surface of positive electrode 202so as to partially or fully cover the surface, may be positioned on aninner surface of the electrode 202 (i.e., adjacent separator 220)instead of the shown outer surface configuration, and/or may beimpregnated or saturated with the positive active material 204 so thatthe reinforcement mat 240 is partially or fully disposed within theactive material 204 layer. Like reinforcement mat 230, reinforcement mat240 also provides additional support to help reduce the negative effectsof shedding of the positive active material particles due to repeatedcharge and discharge cycles.

In some embodiments, reinforcement mat 240 may include a conductivematerial and/or layer to enable electron flow on a surface and/orthrough reinforcement mat 240 to positive terminal 208. In suchembodiments, electrons may flow along either reinforcement mat 240 orgrid/conductor 206 depending on which conductive surface provides anelectrical path of least electrical resistance. For example, electronsproximate to terminal 208 may flow along an electrical path ofgrid/conductor 206 while electrons distal to terminal 208 may flow alongan electrical path of reinforcement mat 240. In some embodiments,reinforcement mat 230 and reinforcement mat 240 may both include aconductive material and/or layer to enable electron flow on or relativeto both mats. Both reinforcement mat 230 and reinforcement mat 240 mayinclude a wetting component as described herein.

With regarding to the reinforcement functions of reinforcement mats 230and/or 240, in some embodiments the reinforcing aspects of these matsmay be enhanced by blending fibers having different fiber diameters.Reinforcement mats 230 and 240 (referred to hereinafter as reinforcementmat 230) can have similar characteristics and compositions, and caninclude a blend of two or more different diameter coarse fibers. In oneembodiment, reinforcement mat 230 includes a plurality of first coarsefibers, having fiber diameters ranging between about 6 μm and about 13μm, between about 6 μm and about 11 μm, or between about 8 μm and about13 μm. The first coarse fibers are blended with a plurality of secondcoarse fibers, having fiber diameters of at least about 6 μm, preferablybetween 6 μm and 7 μm. In some embodiments, the plurality of secondcoarse fibers may include a silane material sizing. The blend of the twoor more different diameter coarse fibers results in a mat that issufficiently strong to structurally support the active material asdescribed above and to withstand the various plate manufacturingprocesses while also minimizing the thickness and overall size of themat. Reducing the thickness of reinforcement mat 230 while maintainingmat strength may be desired since reinforcement mat 230 typically is achemically inactive component and, thus, does not contribute to thebattery's electrochemical process. Reducing the volume of reinforcementmat 230 helps minimize the battery's volume of non-electrochemicallycontributing components.

In one embodiment, reinforcement mat 230 includes a blend of between 10%and 95% of the first coarse fibers and between 5% and 80% of the secondcoarse fibers. In another embodiment, reinforcement mat 230 includes ablend of between 70% and 95% of the first coarse fibers and between 5%and 30% of the second coarse fibers. In another embodiment,reinforcement mat 230 includes a blend of between 40% and 90% of thefirst coarse fibers and between 5% and 30% of the second coarse fibers.In another embodiment, reinforcement mat 230 includes a blend of between10% and 20% of the first coarse fibers and between 60% and 80% of thesecond coarse fibers. In yet another embodiment, the blend of firstcoarse fibers and second coarse fibers is approximately equal (i.e., 50%of the first and second coarse fibers).

The length of the coarse fibers may also contribute to the overallstrength of reinforcement mat 230 by physically entangling with adjacentfibers or fiber bundles and/or creating additional contact points whereseparate fibers are bonded via an applied binder. In one embodiment, thefirst and second coarse fibers have fiber lengths that range betweenabout ⅓ inch and about 1½ inches, although an upper length limit of 1¼inch is more common. This range of lengths provides sufficient matstrength while allowing the fibers to be dispersed in a white watersolution for mat processing applications. In another embodiment, thefirst and second coarse fibers have fiber lengths that range between ½and ¾ of an inch. The fibers lengths of the first coarse fibers may bedifferent than the fibers lengths of the second coarse fibers. Forexample, in one embodiment, the first fibers may have an average fiberlength of about ⅓ inch while the second coarse fibers have an averagefiber length of about ¾inch. In one embodiment, either or both the firstor second coarse fibers have an average fiber length of at least ⅓ inch,while in another embodiment, either or both the first or second coarsefibers have an average fiber length of at least ½ inch.

The type and amount of binder used to bond the first and second coarsefibers together may also contribute to the overall strength andthickness of reinforcement mat 230. As described above, the binder isgenerally an acid and/or chemically-resistant binder that delivers thedurability to survive in the acid environment throughout the life of thebattery, the strength to survive the plate pasting operation, and thepermeability to enable paste penetration. For example, the binder may bean acrylic binder, a melamine binder, a UF binder, or the like. Thebinder may also include and bond the conductive material to the firstand/or second coarse fibers. Increased binder usage may reduce thethickness of reinforcement mat 230 by creating more fiber bonds anddensifying reinforcement mat 230. The increased fibers bonds may alsostrengthen reinforcement mat 230. In one embodiment, the binder isapplied to the first and second coarse fibers such that the bindercomprises between about 5% and 45% by weight of the reinforcement mat230 or between about 15% and 35% by weight of the reinforcement mat. Inanother embodiment, the binder is applied to the first and second coarsefibers such that it comprises between about 5% and 30% by weight of thereinforcement mat 230.

As described herein, the conductive material may be mixed with thebinder or a secondary binder and applied to the first and/or secondcoarse fibers during manufacture of the reinforcement mat 230 orsubsequent thereto. For example, the binder may include conductivefibers (e.g., carbon fibers) and/or other conductive material (e.g.,graphite). In some embodiments, the binder may include between about5-30% graphite particles. The resulting reinforcement mat 230 may havean electrical resistance of less than about 100,000 ohms per square, andmore commonly less than about 50,000 ohms per square, to enable electronflow on a surface of, or through, the reinforcement mat.

The wetting component may be mixed with the binder in some embodiments.The resulting reinforcement mat 230 may have or exhibit an average waterwick height of at least 0.5 cm after exposure to water for 10 minutesconducted according to method ISO8787. The wetting component isdissolvable in an acid solution of the lead-acid battery such that asignificant portion of the nonwoven fiber mat is lost due to dissolvingof the wetting component. For example, between about 5-85% of the massof the reinforcement mat 230 may be lost.

The above described reinforcement mat 230 configurations provide matshaving a total tensile strength of at least 30 lbs/3 inch and morecommonly at least 35 lbs/3 inch. Specifically, the reinforcement mat 230has a tensile strength in the machine direction of at least 22 lbs/3inch and a tensile strength in the cross-machine direction of at least13 lbs/3 inch. The above described mats have been found to havesufficient strength to support the active material and to withstand thevarious stresses imposed during plate or electrode manufacturing andprocessing (e.g., pasting or applying the active material).Reinforcement mat 230 that do not have the above described tensilestrength attributes may not be sufficiently strong to support theapplied active material (e.g., prevent shedding and the like) and/or maypose processing issues, such as mat breakage when applying the activematerial (e.g., lead or lead oxide) paste on the glass mat during theplate reinforcement process.

Further, the above described reinforcement mat 230 configuration providemats that have a thickness of 10 mils or less (i.e., 0.010 inches) andmore commonly 9 mils or less (0.009 inches). In one embodiment, thereinforcement mat 230 have a thickness in the range of between about 6and 8 mils (i.e., 0.006 and 0.008 inches), and preferably about 7 mils.These mats occupy minimal space within the electrode and batteryinterior, which allows for additional electrochemically active materials(e.g., additional electrolyte and/or lead or lead oxide paste) to beincluded in the battery, thereby increasing the life and efficiency ofthe battery. The above described mats have the unique combination ofboth minimal size or thickness and strength while also beingelectrically conductive. The mats may also have a pore size that rangesbetween 50 microns-5 mm.

In some embodiments, separator 220 may have a similar composition asreinforcement mat 230 and may be particularly useful in AGM batteries.For example, separator 220 may be made of glass fibers, or variouspolymers, such as polyethylene, poly propylene, and the like. In someembodiments, the separator 220 may include nonwoven fibers. Theseparator 220 may be a nonwoven fiber mat. In some embodiments, areinforcement mat 250 may be positioned adjacent the separator 220.Separator 220 may have an area weight of between about 100 and 400 g/m².More often, separator 220 has an area weight of between about 150 and300 g/m². The separator 220 may be a mat formed from a combination ofcoarse glass fibers. For example, separator 220 may include a mixture ofbetween about 10-20% of a plurality of first glass fibers havingdiameters of between about 8 and 13 μm and between about 60-80% of aplurality of second glass fibers having diameters at least 6 μm. Theplurality of second glass fibers may include a silane material sizing.Separator 220 may also include an acid resistant binder that bonds thefirst and second plurality of glass fibers to form the separator 220.The binder can be an acrylic binder, melamine binder, UF binder, or thelike. In some embodiments, the separator 220 may include between about70-95% of the mixture of coarse glass fibers. In some embodiments,separator 220 may include 5-30% of an acrylic binder.

In some embodiments, reinforcement mat 250 may also include a conductivematerial and/or layer to enable electron flow on a surface and/orthrough reinforcement mat 250 to positive terminal 208 and/or negativeterminal 218. For example, the fiber mat or mats of reinforcement mat250 may include a conductive material and/or layer, such as within thebinder of the mats, as a film, mat, or layer of conductive fibers,and/or in accordance with any embodiment described herein. For example,the binder may include conductive fibers (e.g., carbon fibers) and/orother conductive materials (e.g., graphite). In such embodiments,electrons may flow along reinforcement mat 230, grid/conductor 216,reinforcement mat 240, grid/conductor 206, separator 220, and/orreinforcement mat 250 depending on which conductive path provides theleast electrical resistance. For example, electrons proximate togrid/conductor 216 may flow along grid/conductor 216 and/orreinforcement mat 230 to terminal 218 while electrons proximate toseparator 220 flow along an electrical path of separator 220 to terminal218. Similarly, electrons proximate to grid/conductor 206 may flow alonggrid/conductor 206 and/or reinforcement mat 240 to terminal 208 whileelectrons proximate to separator 220 flow along an electrical path ofseparator 220 to terminal 208. In such embodiments, the available orpossible electron paths may be greatly increased. In embodiments wherethe separator includes conductive materials, there is a nonconductivelayer and/or other nonwoven nonconductive mat positioned against theconductive portion of the separator. In embodiments not utilizinganother nonwoven nonconductive mat, the conductive mater in theseparator may be positioned on or near a surface of the separator suchthat at least one nonconductive layer extends through a center of theseparator.

In some embodiments, reinforcement mat 250 may also include a wettingcomponent. For example, reinforcement mat 250 may include 10-40% ofcotton fibers, such as cotton microfibers having diameters of betweenabout 0.5 and 3.0 μm. The wetting component may increase thewettability/wickability of the reinforcement mat 250 such that thereinforcement mat 250 has or exhibits an average water wick heightand/or water/acid solution wick height of at least 1.0 cm after exposureto the respective solution for 10 minutes in accordance with a testconducted according to method ISO8787.

Processes and Methods

Referring now to FIG. 4, illustrated is a process 400 for manufacturingan electrode. The process may involve transporting a lead alloy grid 410on a conveyor toward an active material 430 applicator (e.g., lead orlead oxide paste applicator), which applies or pastes the activematerial 430 to the grid 410. A nonwoven mat roll 420 may be positionedbelow grid 410 so that a reinforcement mat is applied to a bottomsurface of the grid 410. The reinforcement mat may include a conductivematerial and/or layer, as well as a wetting component, as describedherein. In some embodiments, the reinforcement mat may also include ablend of coarse fibers as described herein. In some embodiments, thereinforcement mat may also include a blend of coarse and micro glassfibers in addition to the wetting component as described herein. Asecond nonwoven mat roll 440 may be positioned above grid 410 so that asecond reinforcement mat is applied to a top surface of the grid 410.The second reinforcement mat may also include a conductive material, awetting component, and/or layer and/or blend of coarse fibers and/ormicrofibers (similar to or different from reinforcement mat 420). Theresulting electrode or plate 450 may subsequently be cut to length via aplate cutter (not shown). As described herein, the active material 430may be applied to the grid 410 and/or top and bottom of reinforcementmats, 440 and 420, so that the active material impregnates or saturatesthe mats to a desired degree. The electrode or plate 450 may then bedried via a dryer (not shown) or other component of process 400. Asdescribed herein, the reinforcement mats, 440 and 420, may aid in thedrying of the electrode or plate 450 by wicking the water and/orwater/acid solution from the electrode or plate 450 so as to allow thewater and/or water/acid solution to evaporate.

Referring now to FIG. 5, illustrated is a method 500 of manufacturing aplate of a lead-acid battery. At block 510, a grid of lead alloymaterial is provided. The grid of lead alloy material may be either fora positive electrode (e.g., grid/conductor 206) or a negative electrode(e.g., grid/conductor 216) of a battery. At block 520, a paste of activematerial is applied to the grid of lead alloy material to form a batteryplate or electrode (i.e., negative or positive electrode). At block 530,a nonwoven fiber mat is applied to a surface of the paste of the activematerial such that the nonwoven fiber mat is disposed at least partiallywithin the paste of active material. As described herein, the nonwovenfiber mat may include a plurality of fibers, a binder material thatcouples the plurality of fibers together, a wetting component, and aconductive material disposed at least partially within the nonwovenfiber mat so as to contact the paste of active material. The wettingcomponent may provide a wicking capability to allow a complete wettingof the electrodes of a lead-acid battery. The conductive material may beany material described herein and/or a conductive layer that is formedon the nonwoven fiber mat. The nonwoven fiber mat may have an electricalresistant of less than about 100,000 ohms per square to enable electronflow on a surface of the nonwoven fiber mat. In some embodiments, thenonwoven fiber mat may be disposed within the paste of active materialbetween about 0.001 inches and about 0.020 inches.

In some embodiments, the method may also include applying a secondnonwoven fiber mat to an opposite surface of the paste of activematerial so that the grid of lead alloy material is disposed between twononwoven fiber mats. The second nonwoven fiber mat may also contain aconductive material that is disposed at least partially within thesecond nonwoven fiber mat so as to contact the paste of active material.In some embodiments, the nonwoven fiber mat may have a thickness of0.009 inches or less and/or a tensile strength of at least 30 lbs/3inch.

In some embodiments, the plurality of fibers may include a blend ofcoarse fibers as previously described. For example, the plurality offibers may include first fibers having fiber diameters between about 8μm and about 13 μm and second fibers having fiber diameters of at leastabout 6 μm. In some embodiments, the binder may include the conductivematerial. The binder may be applied to the mat between about 5% and 45%by weight, between about 20% and 30% by weight, and the like. In someembodiments, the conductive material may include a plurality ofconductive fibers that are entangled with fibers of the nonwoven fibermat.

Referring now to FIG. 6, illustrated is an embodiment of a method 600 ofmanufacturing a nonwoven fiber mat for reinforcing a plate or electrodeof a lead-acid battery (hereinafter reinforcement mat). The methoddescribed here can be used to produce reinforcement mats for bothflooded lead-acid batteries and for separators in AGM batteries. Atblock 610, a plurality of glass fibers are provided. The glass fibersmay be coarse fibers, microfibers, or a combination of coarse andmicrofibers. At block 620, an acid resistant binder is applied to theplurality of glass fibers to couple the plurality of glass fiberstogether to form the reinforcement mat. At block 630, a wettingcomponent is added to the glass fibers and/or reinforcement mat toincrease the wettability/wickability of the reinforcement mat. Asdescribed herein, the wettability/wickability of the reinforcement matmay be increased such that the reinforcement mat has or exhibits anaverage water wick height and/or average water/acid solution wick heightof at least 0.5 cm after exposure to the respective solution for 10minutes in accordance with the test conducted according to methodISO8787. A conductive material may be applied to the glass fibers and/orreinforcement mat at block 640. Applying the conductive material mayinclude providing a layer of conductive fibers and/or other conductivematerials and positioning this layer atop the glass mat. The conductivematerial may also include a coating that is applied to the mat. In someembodiments, the conductive material may be added to a binder that isapplied to the fiber mat. In other embodiments, the conductive materialmay include conductive fibers that are disposed at least partiallywithin and/or entangled with the fiber mat.

In some embodiments, applying the wetting component includes applyingthe acid resistant binder, where the acid resistant binder includes aconductive material and/or a wettable component (e.g., a hydrophilicfunctional group, a hydrophilic and acid resistant binder mixture, andthe like) that functions to increase the wettability/wickability of thenonwoven fiber mat. In another embodiment, applying the wettingcomponent includes applying a wettable solution (e.g., starch orcellulose solution and the like) to the reinforcement mat such that thewettable solution saturates the reinforcement mat or is disposed on atleast one surface of the reinforcement mat upon drying of the wettablesolution.

In yet another embodiment, applying the wetting component includesbonding a plurality of component fibers (e.g., cellulose fibers and thelike) with the plurality of glass fibers of the reinforcement mat. Insuch embodiments, the reinforcement mat may include between about 40-95%of the glass fibers and up to 50% of the cellulose fibers, and morecommonly between about 10-40% of the cellulose fibers. In a specificembodiment, the reinforcement mat may include between about 60-80% ofthe glass fibers and 10-40% of the cellulose fibers. In still furtherembodiments, applying the wetting component may include applying anycombination of the wetting components described herein, such as thecomponent fibers, wettable solution, and/or acid resistant binder havinga wettable component.

In some embodiments, the plurality of glass fibers may include firstglass fibers having fiber diameters between about 8 μm and about 30 μm.In such embodiments, the method 600 may further include providing aplurality of second glass fibers having fiber diameters between about0.01 μm and about 5 μm and bonding the plurality of second glass fiberswith the first glass fibers via the acid resistant binder. The additionof the second glass fibers may increase the wettability/wickability ofthe reinforcement mat such that the reinforcement mat has or exhibits anaverage water wick height and/or an average water/acid solution wickheight of at least 1.0 cm after exposure to the respective solution for10 minutes in accordance with the test conducted according to methodISO8787. In some embodiments, component fibers (e.g., cellulose fibersand the like) may be bonded with the plurality of first glass fibers andthe plurality of second glass fibers. In such embodiments, thereinforcement mat may include between about 40-80% of the first glassfibers, 10-50% of the second glass fibers, and 5-40% of the cellulosefibers. In another embodiment, the reinforcement mat may include betweenabout 40-50% of the first glass fibers, 20-30% of the second glassfibers, and 20-30% of the cellulose fibers.

Examples

Two reinforcement mats were prepared according to the embodimentsdescribed herein. The resistance of the mats was then measured. Themethods of manufacturing the mats and the results are provided below.

1. Reinforcement Mat Using Graphene as a Conductive Coating

To produce the grapheme conductive coating, a suspension mixture wasprepared using graphene (xGnP-M-15 from XG Sciences) and an acrylicbinder (RHOPLEX™ HA-16 from Dow Chemical). The suspension mixture wasprepared such that it contained approximately 0.5% binder and 1.5%graphene. A spray gun was then used to apply the mixture to a glass mat(Dura-Glass® mat PR-9 and B-10). The mat was then dried at 125 C forapproximately 1 hr and cured at 175 C for approximately 3 mins. Thesurface resistance was then measured and the results are provided inTable 1 below.

TABLE 1 Reinforcement Mat Using Graphene as a Conductive Coating Sam-Surface Weight Surface Sample ple resistivity before resistance lengthwidth (K- coating Graphene Sample (K-Ohm) (cm) (cm) Ohm/sq.) (g) % B-10(1) 1.84 14.3 12.2 1.6 0.7609 15.8% B-10 (2) 3.41 14.2 12.2 2.9 0.764314.5% B-10 (3) 2.25 14.2 11.9 1.9 0.7334 17.3% PR-9 (1) 13.76 14.2 1211.6 0.4577 10.1% PR-9 (2) 18.26 14.2 12.3 15.8 0.4651 11.7% PR-9 (3)5.29 14.7 12.2 4.4 0.4728 8.9%

By using the graphene material, a significant weight loss of the coatingafter a standard acid test (40 wt. % sulfuric acid, 70 C for 72 hrs) wasnot exhibited or experienced. As such, the graphene coated glass matsexperience similar weight loss as uncoated glass mats. However, a slightdrop in conductivity was observed after the mat was exposed to sulfuricacid for an extended time. This slight drop in conductivity may indicatereaction between the graphene and sulfuric acid.

2. Reinforcement Mat Using CNS (Carbon Nanostructure) as a ConductiveCoating

To produce the CNS conductive coating, a suspension mixture was preparedusing CNS (from Applied Nanostructured Solutions LLC) and/or an acrylicbinder (RHOPLEX™ HA-16 from Dow Chemical). The suspension mixture wasprepared such that it contained approximately 1% binder (or no binder)and 0.5% CNS. A glass mat (Dura-Glass® mat PR-9 or uncoated polyesterspunbond mat) was placed in the mixture and water was vacuumed out. Auniform coating of the CNS was obtained. The mat was then dried at 125 Cfor approximately 1 hr and cured at 175 C for approximately 3 mins. Thesurface resistance was then measured and the results are provided inTable 2 below.

TABLE 2 Reinforcement Mat Using CNS (Carbon Nanostructure) as aConductive Coating Surface Sample Sample Surface resistance length widthresistivity Com- Sample (Ohm) (inch) (inch) (Ohm/sq.) CNS % ment PR-9(1) 180 14 12 154.3 2.50%   With binder PR-9 (2) 65 14 14 65.0 15%Without binder PR-9 (3) 53 14 14 53.0 25% With binder PR-9 (4) 50 14 1450.0 15% Without binder PR-9 (5) 66 14 14 66.0 25% Without binderPolyester 239 13.5 13.5 239.0 0.3%  With (1) binder Polyester 68 13.513.5 68.0  2% With (2) binder Polyester 132 13.5 13.5 132.0 0.66%   With(2) binder

By using the CNS material, a significant weight loss of the coatingafter a standard acid test (40 wt. % sulfuric acid, 70 C for 72 hrs) wasnot exhibited or experienced. As such, the CNS coated glass matsexperience similar weight loss as uncoated glass mats. In addition, asignificant drop in conductivity was not observed after the mat wasexposed to sulfuric acid for an extended time. It is believed that sincethe CNS has the structure of a “crosslinked matrix of carbon nanotubes,”even though sulfuric acid attacks some carbon, the whole structureremains connected and, thus, the conductivity of the coating is notaffected. Given these results, CNS may be a better choice as aconductive coating than graphene. Further, the CNS coating provides amuch better conductivity (i.e., less resistance) than graphene onnon-woven mats. For example, as shown in Table 1, K-ohm units are usedfor graphene resistance, whereas in Table 2, Ohm units are used for CNSresistance.

Several reinforcement mats were manufactured in accordance with theembodiments described herein and tested to determine thewettability/wickability of the mats. The wettability/wickability testswere conducted according to method ISO8787. The mats were exposed toboth a water solution and a water/acid solution where the concentrationof sulfuric acid was approximately 40%. The results of the tests areshown in Table 3 below.

TABLE 3 Sample Reinforcement Mat Average Average acid water wickingwicking (40%) height height after after Sample Sample 10 mins Std 10mins Std ID description Binder (cm) Dev (cm) Dev Control 100% RHOPLEX ™0.0 0 0.0 0.0 coarse HA-16 glass fibers 1 50% ¾″ RHOPLEX ™ 0.8 0.15 1.20.12 K249 T, HA-16 50% cellulose 2 50% ¾″ Hycar ® FF 0.9 0.15 0.9 0.15K249 T, 26903 50% cellulose 3 50% ¾″ Hycar ® FF 2.7 0.05 1.9 0.25 K249T, 26903 25% cellulose, 25% 206-253

A control mat was also manufactured and tested to provide a comparisonor reference point for the other tested mats. The control mat includes100% coarse glass fibers (T glass fibers) having an average fiber lengthof approximately ¾″ and an average fiber diameter of approximately 13μm. The glass fibers were bonded together with an acid resistant bindersold by Dow Chemical under the trade name RHOPLEX™ HA-16. The acidresistant binder was applied so as to have a Loss on Ignition (LOI) ofapproximately 20%. The control mat exhibited an average water wickingheight and an average acid wicking height of approximately 0.0 cm afterexposure to the respective solutions for 10 minutes. Stated differently,the control mat exhibited essentially no wettability/wickability.

A first mat (i.e. Sample ID 1) was manufactured to include approximately50% coarse glass fibers having an average fiber length of approximately¾″ and an average fiber diameter of approximately 13 μm and to include50% cellulose fibers having an average fiber length of approximately2.40 mm. The cellulose fibers were made from a pulp slurry bypre-soaking a Kraft board in water (e.g., Kamloops Chinook Kraft boardmanufacture by Domtar) and stirring the soaked Kraft board in water forat least 10 minutes. The cellulose fiber pulp slurry was then combinedwith the glass fibers. The coarse glass fibers and cellulose fibers werebond together with the RHOPLEX™ HA-16 binder so as to have an LOI ofapproximately 20%. The first mat exhibited an average water wickingheight of approximately 0.8 cm with a standard deviation of 0.15 afterexposure to the water solution for 10 minutes. The first mat alsoexhibited an average water/acid solution wicking height of approximately1.2 cm with a standard deviation of 0.12 after exposure to thewater/acid solution for 10 min.

A second mat (i.e. Sample ID 2) was manufactured to includeapproximately 50% coarse glass fibers and 50% cellulose fibers havingfiber properties similar to the first mat. The coarse glass fibers andcellulose fibers were bond together with an acid resistant binder soldby Lubrizol under the trade name Hycar® FF 26903. The binder was appliedso as to have an LOI of approximately 20%. The second mat exhibited anaverage water wicking height of approximately 0.9 cm with a standarddeviation of 0.15 after exposure to the water solution for 10 minutes.The second mat also exhibited an average water/acid solution wickingheight of approximately 0.9 cm with a standard deviation of 0.15 afterexposure to the water/acid solution for 10 min.

A third mat (i.e. Sample ID 3) was manufactured to include approximately50% coarse glass fibers and 25% cellulose fibers having fiber propertiessimilar to the first and second mats. The third mat also includedapproximately 25% glass microfibers having an average fiber diameter ofapproximately 0.76 μm (i.e., Johns Manville 206-253 fibers). The coarseglass fibers, glass microfibers, and cellulose fibers were bond togetherwith the Hycar® FF 26903 binder so as to have an LOI of approximately20%. The third mat exhibited an average water wicking height ofapproximately 2.7 cm with a standard deviation of 0.05 after exposure tothe water solution for 10 minutes. The third mat also exhibited anaverage water/acid solution wicking height of approximately 1.9 cm witha standard deviation of 0.25 after exposure to the water/acid solutionfor 10 min.

As shown in the test results above, the addition of the wettingcomponent to the reinforcement mat, which in this case includedcellulose fibers, significantly increased the wettability/wickability ofthe reinforcement mat. Further, the inclusion of glass microfibers inthe reinforcement mat in addition to the wetting component significantlyincreased the wettability/wickability of the reinforcement mat beyondthat exhibited by adding the wetting component alone.

Having described several embodiments, it will be recognized by those ofskill in the art that various modifications, alternative constructions,and equivalents may be used without departing from the spirit of theinvention. Additionally, a number of well-known processes and elementshave not been described in order to avoid unnecessarily obscuring thepresent invention. Accordingly, the above description should not betaken as limiting the scope of the invention.

Where a range of values is provided, it is understood that eachintervening value, to the tenth of the unit of the lower limit unlessthe context clearly dictates otherwise, between the upper and lowerlimits of that range is also specifically disclosed. Each smaller rangebetween any stated value or intervening value in a stated range and anyother stated or intervening value in that stated range is encompassed.The upper and lower limits of these smaller ranges may independently beincluded or excluded in the range, and each range where either, neitheror both limits are included in the smaller ranges is also encompassedwithin the invention, subject to any specifically excluded limit in thestated range. Where the stated range includes one or both of the limits,ranges excluding either or both of those included limits are alsoincluded.

As used herein and in the appended claims, the singular forms “a”, “an”,and “the” include plural referents unless the context clearly dictatesotherwise. Thus, for example, reference to “a process” includes aplurality of such processes and reference to “the device” includesreference to one or more devices and equivalents thereof known to thoseskilled in the art, and so forth.

Also, the words “comprise,” “comprising,” “include,” “including,” and“includes” when used in this specification and in the following claimsare intended to specify the presence of stated features, integers,components, or steps, but they do not preclude the presence or additionof one or more other features, integers, components, steps, acts, orgroups.

What is claimed is:
 1. An absorptive glass mat (AGM) battery comprising:a positive electrode; a negative electrode; a nonwoven fiber matseparator positioned between the positive electrode and the negativeelectrode, the nonwoven fiber separator comprising: a mixture of glassfibers comprising: a plurality of first glass fibers having diametersbetween about 8 μm to 13 μm; and a plurality of second glass fibershaving diameters of at least 6 μm, the plurality of second glass fiberscomprising a silane material sizing; an acid resistant binder that bondsthe plurality of first and second glass fibers to form the nonwovenfiber separator; a wetting component applied to the nonwoven fiberseparator to increase the wettability of the nonwoven fiber separatorsuch that the nonwoven fiber separator has or exhibits an average waterwick height of at least 1.0 cm after exposure to water for 10 minutesconducted according to method ISO8787; and a conductive materialdisposed on at least one surface of the nonwoven fiber separator suchthat when the nonwoven fiber separator is positioned adjacent thepositive or negative electrode, the conductive material contacts thepositive or the negative electrode, the nonwoven fiber separator havingan electrical resistance of less than about 100,000 ohms per square toenable electron flow about the nonwoven fiber separator.
 2. Thelead-acid battery according to claim 1, wherein the mixture of glassfibers comprises between about 10% to 20% of the first glass fibers andbetween about 60% to 80% of the second glass fibers.
 3. The lead-acidbattery according to claim 1, wherein the nonwoven fiber separator hasan area weight of between about 100 g/m² and about 400 g/m².
 4. Thelead-acid battery according to claim 1, wherein the wetting componentcomprises one or more of cotton fibers, cellulose fibers, or polyesterfibers that are bonded with the nonwoven fiber separator.
 5. Thelead-acid battery according to claim 4, wherein the one or more ofcotton fibers, cellulose fibers, or polyester fibers form a mat that isbonded to at least one side of the nonwoven fiber separator.
 6. Thelead-acid battery according to claim 4, wherein the one or more ofcotton fibers, cellulose fibers, or polyester fibers are entangled withthe mixture of coarse glass fibers to form the nonwoven fiber separator.7. The lead-acid battery according to claim 1, wherein the bindercomprises a plurality of conductive fibers or conductive particles. 8.The lead-acid battery according to claim 1, wherein the conductivematerial comprises a plurality of carbon fibers that are entangled withthe mixture of coarse glass fibers of the nonwoven fiber separator.
 9. Anonwoven fiber separator for an AGM battery, the nonwoven fiberseparator comprising: a mixture of glass fibers comprising: a pluralityof first glass fibers having diameters between about 8 μm to 13 μm; anda plurality of second glass fibers having diameters of at least 6 μm,the plurality of second glass fibers comprising a silane materialsizing; an acid resistant binder that bonds the plurality of first andsecond glass fibers to form the nonwoven fiber separator; a wettingcomponent applied to the nonwoven fiber separator to increase thewettability of the nonwoven fiber separator such that the nonwoven fiberseparator has or exhibits an average water wick height of at least 1.0cm after exposure to water for 10 minutes conducted according to methodISO8787; and a conductive material disposed on at least one surface ofthe nonwoven fiber separator at such that when the nonwoven fiberseparator is positioned adjacent a positive or a negative electrode of alead-acid battery, the conductive material contacts the positive ornegative electrode, the nonwoven fiber separator having an electricalresistance of less than about 100,000 ohms per square to enable electronflow about the nonwoven fiber separator.
 10. The nonwoven fiberseparator according to claim 9, wherein the nonwoven fiber separator hasan area weight of between about 150 g/m² and about 300 g/m².
 11. Thenonwoven fiber separator according to claim 9, wherein the wettingcomponent comprises cotton fibers having diameters between about 0.5 μmto 3 μm.
 12. The nonwoven fiber separator according to claim 9, whereinthe nonwoven fiber separator comprises between about 70% to 95% of themixture of coarse glass fibers and between about 5% to 30% of thebinder.
 13. The nonwoven fiber separator according to claim 9, whereinthe mixture of glass fibers comprises between about 10% to 20% of thefirst glass fibers and between about 60% to 80% of the second glassfibers.
 14. The nonwoven fiber separator according to claim 9, whereinthe conductive material further comprises carbon fibers that are betweenabout 8 mm to 12 mm in length and having diameters between about 6 μm to10 μm.
 15. The nonwoven fiber separator according to claim 9, whereinthe binder comprises one or more of acrylic, melamine, phenolic, or ureaformaldehyde (UF) binders.
 16. A method of manufacturing a nonwovenfiber separator for use in a lead-acid battery, the method comprising:providing a mixture of glass fibers comprising: a plurality of firstglass fibers having diameters between about 8 μm to 13 μm; and aplurality of second glass fibers having diameters of at least 6 μm, theplurality of second glass fibers comprising a silane material sizing;applying an acid resistant binder to the mixture of glass fibers tocouple the mixture of glass fibers together to form the nonwoven fiberseparator; applying a conductive material to at least one surface of thenonwoven fiber separator such that when the nonwoven fiber separator ispositioned adjacent a positive or a negative electrode of a battery, theconductive material contacts the positive or the negative electrode, thenonwoven fiber separator having an electrical resistance of less thanabout 100,000 ohms per square so as to enable electron flow about thenonwoven fiber separator; and applying a wetting component to thenonwoven fiber separator to increase the wettability of the nonwovenfiber separator such that the nonwoven fiber separator has or exhibitsan average water wick height of at least 1.0 cm after exposure to waterfor 10 minutes conducted according to method ISO8787.
 17. The method ofclaim 16, wherein the nonwoven fiber separator has an area weight ofbetween about 150 g/m² and about 300 g/m².
 18. The method of claim 16,wherein the nonwoven fiber separator comprises between about 10% to 40%of the wetting component.
 19. The method of claim 16, wherein applyingthe wetting component comprises bonding one or more of cotton fibers,cellulose fibers, or polyester fibers with the mixture of coarse glassfibers of the nonwoven fiber separator.
 20. The method of claim 16,wherein the conductive material comprises one or more of graphite fibersor carbon fibers.